نتایج جستجو برای: α1 antitrypsin a1at

تعداد نتایج: 9172  

2015
Shaowei Wang Jingming Zhou Xiaochun Wei Pengcui Li Kai Li Dongming Wang Fangyuan Wei Jianzhong Zhang Lei Wei

Western blot of synovial fluid has been widely used for osteoarthritis (OA) research and diagnosis, but there is no ideal loading control for this purpose. Although β-actin is extensively used as loading control in western blot, it is not suitable for synovial fluid because it is not required in synovial fluid as a cytoskeletal protein. A good loading control for synovial fluid in OA studies sh...

2017
Karina A Serban Daniela N Petrusca Andrew Mikosz Christophe Poirier Angelia D Lockett Lauren Saint Matthew J Justice Homer L Twigg Michael A Campos Irina Petrache

Cigarette smoking (CS), the main risk factor for COPD (chronic obstructive pulmonary disease) in developed countries, decreases alveolar macrophages (AM) clearance of both apoptotic cells and bacterial pathogens. This global deficit of AM engulfment may explain why active smokers have worse outcomes of COPD exacerbations, episodes characterized by airway infection and inflammation that carry hi...

2015
BO-YUN JANG HYUNG DON RYOO JAEKYOUNG SON KYUNG-CHUL CHOI DONG-MYOUNG SHIN SANG-WOOK KANG MIN-JI KANG

The synthesis of proteins in the endoplasmic reticulum (ER) that exceeds the protein folding capacity of this organelle is a frequent cause of cellular dysfunction and disease. An example of such a disease is alpha-1-antitrypsin (A1AT) deficiency, caused by destabilizing mutations in this glycoprotein. It is considered that the mutant proteins are recognized in the ER by lectins and are subsequ...

2016
Phyllis M. Quinn David W. Dunne Shona C. Moore Richard J. Pleass

Several splice variants of IgE exist in human plasma, including a variant called IgE-tailpiece (IgE-tp) that differs from classical IgE by the replacement of two carboxy-terminal amino acids with eight novel residues that include an ultimate cysteine. To date, the role of the secreted IgE-tp isoform in human immunity is unknown. We show that levels of IgE-tp are raised in helminth-infected dono...

2002
D Yoon F Kueppers R M Genta G B Klintmalm V I Khaoustov B Yoffe

Background: Alpha-1-antitrypsin (A1AT) deficiency is the most common inherited metabolic disorder with the potential to cause injury in the lung and liver. Recent reports suggested that alpha-1-antichymotrypsin (A1AC) deficiency may also be a possible cause of chronic liver disease. However, it has received little attention and is rarely investigated in the clinical setting. Aims: To assess the...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2013
Ahmed Fahim Rachel Wilmot Simon Paul Hart

A 47-year-old Caucasian male presented to the chest clinic with a 4-week history of exertional dyspnea. A chest radiograph showed mild hyperinflation without any focal pathology and spirometry showed a mild obstructive defect. In view of symptoms being disproportionate to spirometric and radiologic abnormalities, a thoracic CT scan was obtained. It revealed that there was evidence of bronchiect...

2006
E C KLASEN

Ninety-three Spanish children suffering from coeliac disease and 103 control subjects from the same area were screened for the amount of ao1-antitrypsin (oc1AT) and for any electrophoretic variations in it. In this case-control study no significant differences were detected either in phenotype distribution or amount. The present results indicate that no genetic association exists between a1AT a...

Journal: :Journal of The National Comprehensive Cancer Network 2023

Hepatobiliary cancers are aggressive tumors that affect the liver and biliary tract responsible for nearly 550,000 deaths per year. The most common malignancy is hepatocellular carcinoma, risk factors include viral hepatitis infection, nonalcoholic steatohepatitis, excessive alcohol use. Other etiologies Wilson’s disease, α1-antitrypsin deficiency, cryptogenic cirrhosis. Clinicians should be aw...

Journal: :Clinical chemistry 2011
Yuhong Chen Melissa R Snyder Yi Zhu Linda J Tostrud Linda M Benson Jerry A Katzmann H Robert Bergen

BACKGROUND α-1-Antitrypsin (A1AT) deficiency results from a genetic disorder at 2 common loci. Diagnosis requires quantification of A1AT and subsequent identification of the specific variant. The current algorithm of laboratory testing for the diagnosis of A1AT deficiency uses a combination of quantification (nephelometry), genotyping, and/or phenotyping. We developed a multiple reaction monito...

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